List of variants in gene combination ANK1, LOC126860368 reported as uncertain significance for anemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.4448T>G (p.Leu1483Arg)	rs141408004	0.00043
NM_000037.4(ANK1):c.4472G>A (p.Arg1491His)	rs372878614	0.00004
NM_000037.4(ANK1):c.4427G>T (p.Arg1476Leu)
NM_000037.4(ANK1):c.4444A>G (p.Met1482Val)	rs2150578454
NM_000037.4(ANK1):c.4492C>T (p.Arg1498Trp)
NM_000037.4(ANK1):c.4497C>T (p.His1499=)	rs370037242
NM_000037.4(ANK1):c.4501G>C (p.Asp1501His)
NM_000037.4(ANK1):c.4524C>T (p.Pro1508=)	rs886062938

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